BSI The Netherlands hosts our first MDR Webinar Series for the consulting community, providing key insights into regulatory and compliance expectations for CE marking for medical devices.
Meet Our Experts
Join our two interactive sessions with experts Richard Holborow, Diego Falletti, Kevin Madden and Dörte Asmus to discuss lessons learnt around Post Market Serveillance, Clinical Evaluation and Technical Documentation under the MDR.
BSI The Netherlands is a leading EU Notified Body; we review technical documentation as part of a conformity assessment to ensure that medical devices meet the necessary safety and performance requirements to allow them to be placed on the market.